Yamane & Wang, W., 2015
Yamane and Wang (2015) - Specimens were collected in the daytime from a bivouac in soil, obscured by networks of tree roots, in a primary lowland dipterocarp forest. Collection was made in July 2012, a month of supposed relatively low rainfall, just before the low rainfall (dry) season of August – September in Danum Valley (Walsh & Newbery 1999).
- 1 Identification
- 2 Distribution
- 3 Biology
- 4 Castes
- 5 Nomenclature
- 6 References
- 7 References based on Global Ant Biodiversity Informatics
Yamane and Wang (2015) - Aenictus sirenicus belongs to the Aenictus pachycerus species group that has a very wide distribution range from Sri Lanka through Indochina and the Sunda region to Australia (Jaitrong &Yamane 2011). The present species is, however, exceptional among members of this group. The body is very slender, with an exceptionally elongate petiole that is almost twice as long as high in profile. The mandible is more slender than usual, almost entirely smooth and shiny, with the basal margin bearing several small denticles. The clypeus is more strongly produced anteriorly with a rather pointed apex. The frontal ridges are short, parallel to each other, and do not merge into a single carina. The parafrontal ridges are poorly developed, only reaching the posterior margin of the antennal sockets.
In Borneo three species of the A. pachycerus group, i.e., Aenictus dentatus, Aenictus kutai and Aenictus levior have been recorded (Jaitrong & Wiwatwitaya 2013). The present newly described species resembles neither of these, and seems not to have any closely related species in other parts of the range of this group. Three Philippine species, Aenictus carolianus, Aenictus powersi and Aenictus reyesi have smooth heads but have densely sculptured mandibles and other character conditions shared by the remaining species of the group (Wilson 1964; Zettel & Sorger 2010).
Keys including this Species
Sabah, Borneo (E. Malaysia).
Distribution based on Regional Taxon Lists
Distribution based on AntMaps
Distribution based on AntWeb specimens
Check data from AntWeb
Yamane and Wang (2015) - Aenictus sirenicus is known only from the type series collected in Danum Valley, Lahad Datu, Sabah. Another strange Bornean species, Aenictus inflatus Yamane et Hashimoto (the only member of the A. inflatus group), has also been collected from a single locality, Lambir Hills National Park, Sarawak (Yamane & Hashimoto 1999). At present it is not certain if these are endemic species specialized to particular localities in Borneo or represent relict species that have become extinct in other places. Exploring primary forests that have been untouched by myrmecologists will likely reveal more unnamed Aenictus species in Borneo.
Little is known about the biology of Aenictus sirenicus. The genus is comprised of species that live an army ant lifestyle. Aenictus typically prey on other ants, from other genera, or other insects such as wasps or termites. There are reports of Aenictus preying on other insects as well and even have been observed collecting honeydew from homopterans (Santschi, 1933; Gotwald, 1995) but this appears, at least from available evidence, to be uncommon. Foraging raids can occur day or night across the ground surface. Occasionally raids are arboreal. During a raid numerous workers attack a single nest or small area, with several workers coordinating their efforts to carry large prey items back to the nest or bivouac. Aenictus have a nomadic life style, alternating between a migratory phase in which nests are temporary bivouacs in sheltered places above the ground and a stationary phase where semi-permanent underground nests are formed. During the nomadic phase bivouacs move regularly, sometimes more than once a day when larvae require large amounts of food. Individual nests usually contain up to several thousand workers, although nest fragments containing only a few hundred workers are often encountered. Queens are highly specialised and look less like workers than in most ant species. They have greatly enlarged gasters (dichthadiform) and remain flightless throughout their life. New colonies are formed by the division of existing colonies (fission) rather than by individual queens starting colonies on their own.
The following information is derived from Barry Bolton's Online Catalogue of the Ants of the World.
- sirenicus. Aenictus sirenicus Yamane & Wang, 2015: 53, figs. 1, 2 (w.) BORNEO (East Malaysia: Sabah).
- Type-material: holotype worker, 7 paratype workers.
- Type-locality: holotype Malaysia: Borneo, Sabah, Danum Valley, Lahad Datu Dist., vii.2012, BRL2WF3 (W. Wang); paratypes with same data.
- Type-depositories: MBSM (holotype); MBSM, SKYC, TNHM (paratypes).
- Distribution: Malaysia (Sabah).
Unless otherwise noted the text for the remainder of this section is reported from the publication that includes the original description.
Six workers measured (holotype in parentheses). Total body length: 3.3-3.6 (3.3), head width (HW): 0.60-0.64 (0.60), head length (HL): 0.80-0.82 (0.82), scape length (SL): 0.66-0.74 (0.72), petiolar length: 0.40-0.42 (0.40), petiolar height: 0.22-0.24 (0.22), petiolar width: 0.15-0.16 (0.15), postpetiolar length: 0.32-0.36 (0.32), postpetiolar height: 0.22-0.24 (0.22), postpetiolar width: 0.16-0.18 (0.17), Cephalic index (HW × 100 / HL): 73.0-80.0 (73.0), Scape index (SI × 100 / HW): 106-120 (120).
In full-face view head distinctly longer than broad, with nearly straight posterior margin; its sides parallel in anterior half, then weakly converging posteriad; occipital carina low, absent on most part of gena. Frontal carinae continuous from rims forming posterior margin of clypeus, parallel, close to each other but not merging into a single carina, short, only reaching posterior margin of antennal sockets. Parafrontal ridge ill-developed, low and short. Clypeus composed of steeply sloping posterior half and triangularly produced anterior half that is lamellate. Mandible broadest at 3/5 length from base; masticatory margin weakly concave, with a pointed apical tooth that is very large so that its apex is very far from first denticle on masticatory margin (inner margin with a relatively long diastema); masticatory margin with 5-6 denticles including basal tooth; basal margin with several minute denticles. Antenna 10-segmented; scape when laid back almost attaining posterior margin of head; all flagellar segments longer than broad; antennal segment 3 longer than 2 and 4; apical segment long, 1.5 times as long as the preceding segment, apically sharply pointed. Mesosoma elongate, slightly longer than gaster; in profile pronotum higher posteriorly; weak indentation present between pronotum and mesonotum; mesonotum weakly convex, slightly higher than propodeum; dorsum of propodeum almost flat; propodeal declivity short and small, margined from lateral and dorsal faces with well-developed carina (wall); mesopleuron demarcated from metapleuron by deep furrow that extends anteriad up to base of fore coxa; light-colored round area present at lowermost part of mesopleuron just above mid-coxa. Propodeal spiracle small, located at posterior end of elongate tubercle, far from metanotal gland orifice; the tubercle very prominent seen from above. Petiole elongate, in profile slightly less than twice as long as high, higher posteriorly, without subpetiolar process; ventral margin weakly convex; posterior face of node vertical, margined by weak carina; postpetiole shorter than and as high as petiole, in profile with anteroventral acute process and concave ventral margin; posterior face of node steep, not margined by carina. Gastral tergite 1 (abdominal tergite 4) distinctly longer than broad, much larger than remaining tergites.
Head capsule and mandible extensively smooth and shiny; clypeus entirely finely and densely sculptured and dull; antennal scape densely sculptured with fine, superficial punctures and very weakly shiny; flagellar segments densely sculptured with fine granules, and dull. Pronotal dorsum smooth and shiny; lateral face of pronotum and mesonotum with superficial punctation; posterior half of mesosoma more strongly sculptured. Petiole extensively and finely sculptured, with dorsum often smoother; dorsum of postpetiole almost smooth and shiny; other parts of postpetiole sculptured. Coxae, femora and tibiae superficially sculptured and weakly shiny; tarsi more distinctly microsculptured and dull. Gaster smooth and shiny.
Dorsum of head and pronotum sparsely covered with rather long hairs that are slightly shorter than the apical segment of antenna, mixed with much shorter hairs. Mesonotum, propodeum, waist, and gastral tergites and sternites more densely covered with standing hairs that are shorter than sparse long hairs on head dorsum. Outer face of mandible and antennal scape with standing hairs of variable length; flagellar segments with much shorter hairs; apical segment densely covered with erect pubescence, without standing hairs. Legs with standing hairs of variable length.
Body rather distinctly bicoloured; head, antenna, waist, gaster and legs yellowish to light brown or orange; vertex of head darker; mesosoma blackish except for dorsum and ventral margin of pronotum yellowish brown.
Holotype: worker, Danum Valley, Lahad Datu District, Sabah, Borneo (E. Malaysia) (5°1.03’N; 117°44.87’E) vii 2012, leg. W. Wang, BRL2WF3 Aii (Institute for Tropical Biology and Conservation: Malaysia Sabah University). Paratypes: 7 workers, same data as above (SKY Collection, Kitakyushu Museum of Natural History and Human History; Thailand Natural History Museum; ITBC).
The specific epithet sirenicus means “bewitching” in Latin, and refers to the attractive body proportion and coloration of the new species.
- Yamane, S. & Wang, W. 2015. Description of a new species of the Aenictus pachycerus group from Borneo. Asian Myrmecology. 7:53-56.
References based on Global Ant Biodiversity Informatics
- Borowiec M. L. 2016. Generic revision of the ant subfamily Dorylinae (Hymenoptera, Formicidae). ZooKeys 608: 1–280.